U.S. patent application number 15/945405 was filed with the patent office on 2019-01-24 for reversible electrochemical mirror.
This patent application is currently assigned to ELECTRONICS AND TELECOMMUNICATIONS RESEARCH INSTITUTE. The applicant listed for this patent is ELECTRONICS AND TELECOMMUNICATIONS RESEARCH INSTITUTE. Invention is credited to Chil Seong AH, Sang Hoon CHEON, Seong-Mok CHO, Chi-Sun HWANG, Joo Yeon KIM, Sujung KIM, Tae-Youb KIM, Yong Hae KIM, Jeong Ik LEE, Hojun RYU, Juhee SONG.
Application Number | 20190025665 15/945405 |
Document ID | / |
Family ID | 64951478 |
Filed Date | 2019-01-24 |
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United States Patent
Application |
20190025665 |
Kind Code |
A1 |
CHO; Seong-Mok ; et
al. |
January 24, 2019 |
REVERSIBLE ELECTROCHEMICAL MIRROR
Abstract
Provided is a reversible electrochemical mirror including a
first substrate and a second substrate, which face each other, a
first transparent electrode disposed on the first substrate and
facing the second substrate, a second transparent electrode
disposed on the second substrate and facing the first transparent
electrode, an electrolyte solution interposed between the first
transparent electrode and the second transparent electrode, and a
counter electrode material layer disposed on the second transparent
electrode and contacting the electrolyte solution.
Inventors: |
CHO; Seong-Mok; (Daejeon,
KR) ; KIM; Sujung; (Daejeon, KR) ; KIM;
Tae-Youb; (Daejeon, KR) ; SONG; Juhee;
(Daejeon, KR) ; AH; Chil Seong; (Daejeon, KR)
; KIM; Yong Hae; (Daejeon, KR) ; KIM; Joo
Yeon; (Daejeon, KR) ; RYU; Hojun; (Seoul,
KR) ; LEE; Jeong Ik; (Daejeon, KR) ; CHEON;
Sang Hoon; (Daejeon, KR) ; HWANG; Chi-Sun;
(Daejeon, KR) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
ELECTRONICS AND TELECOMMUNICATIONS RESEARCH INSTITUTE |
Daejeon |
|
KR |
|
|
Assignee: |
ELECTRONICS AND TELECOMMUNICATIONS
RESEARCH INSTITUTE
Daejeon
KR
|
Family ID: |
64951478 |
Appl. No.: |
15/945405 |
Filed: |
April 4, 2018 |
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
G02F 2001/1555 20130101;
G02F 1/19 20130101; G02F 2201/12 20130101; G02F 1/163 20130101 |
International
Class: |
G02F 1/19 20060101
G02F001/19 |
Foreign Application Data
Date |
Code |
Application Number |
Jul 21, 2017 |
KR |
10-2017-0092951 |
Claims
1. A reversible electrochemical mirror comprising: a first
substrate and a second substrate, which face each other; a first
transparent electrode disposed on the first substrate and facing
the second substrate; a second transparent electrode disposed on
the second substrate and facing the first transparent electrode; an
electrolyte solution interposed between the first transparent
electrode and the second transparent electrode; and a counter
electrode material layer disposed on the second transparent
electrode and contacting the electrolyte solution.
2. The reversible electrochemical mirror of claim 1, wherein the
counter electrode material layer includes an ion storage material
or an electrochromic material.
3. The reversible electrochemical mirror of claim 1, wherein the
counter electrode material layer includes at least one out of
tungsten oxide (WO.sub.3), cerium oxide (CeO.sub.2), titanium oxide
(TiO.sub.2), nickel oxide (NiO), molybdenum oxide (MoO.sub.3),
cobalt oxide (CoO.sub.2), iridium oxide (IrO.sub.2), and tin oxide
(SnO.sub.2).
4. The reversible electrochemical mirror of claim 1, further
comprising a metal layer disposed on the first transparent
electrode and contacting the electrolyte solution.
5. The reversible electrochemical mirror of claim 4, wherein the
electrolyte solution includes ions of a metal included in the metal
layer.
6. The reversible electrochemical mirror of claim 5, wherein the
metal layer includes silver (Ag) or bismuth (Bi), and the
electrolyte solution includes silver ions or bismuth ions.
7. The reversible electrochemical mirror of claim 6, wherein the
electrolyte solution further includes lithium ions.
8. The reversible electrochemical mirror of claim 5, wherein the
electrolyte solution further includes at least one solvent selected
from water, dimethyl sulfoxide (DMSO), propylene carbonate, and
ethylene glycol.
9. The reversible electrochemical mirror of claim 1, wherein the
electrolyte solution does not include copper ions.
10. The reversible electrochemical mirror of claim 1, wherein the
first and second transparent electrodes include ITO or FTO.
11. The reversible electrochemical mirror of claim 1, wherein, when
a negative voltage is applied to the first transparent electrode, a
metal layer is electrodeposited on the first transparent electrode
such that the reversible electrochemical mirror becomes a mirror
state, and when a negative voltage is applied to the second
transparent electrode, the metal layer dissolves into the
electrolyte solution such that the reversible electrochemical
mirror becomes a transparent state.
Description
CROSS-REFERENCE TO RELATED APPLICATION
[0001] This U.S. non-provisional patent application claims priority
under 35 U.S.C. .sctn. 119 of Korean Patent Application No.
10-2017-0092951, filed on Jul. 21, 2017, the entire contents of
which are hereby incorporated by reference.
BACKGROUND
[0002] The present disclosure herein relates to a reversible
electrochemical mirror.
[0003] Reversible electrochemical mirrors using reversible
electrodeposition techniques are devices that can be reversibly
transformed between mirror and transparent states through a method
in which metals, such as silver (Ag) or bismuth (Bi) and the like,
are electrodeposited on or removed from a transparent electrode
through electrochemical methods. Due to having the innate property
of mirror/transparent state transformation, reversible mirrors
based on reversible electrodeposition techniques are expected to be
utilized in various ways, for instance, as smart windows or as
design devices in electronic products and the like.
[0004] Such reversible electrochemical mirrors based on reversible
electrodeposition techniques are typically configured to have an
electrolyte positioned between two substrates including electrodes.
The reversible electrochemical mirror may become either a mirror or
transparent as metal ions dissolved in the electrolyte are either
electrodeposited or re-dissolved depending on whether or not
voltage is applied to the electrodes.
[0005] In typical reversible electrochemical mirrors, voltage must
be continuously applied to maintain the mirror state, and thus
there are limitations in that power consumption is significant and
increasing the surface of the mirrors is difficult.
SUMMARY
[0006] The present disclosure provides a method for manufacturing a
reversible electrochemical mirror that can be operated at low power
and exhibits excellent performance.
[0007] An embodiment of the inventive concept provides a reversible
electrochemical mirror including a first substrate and a second
substrate, which face each other; a first transparent electrode
disposed on the first substrate and facing the second substrate; a
second transparent electrode disposed on the second substrate and
facing the first transparent electrode; an electrolyte solution
interposed between the first transparent electrode and the second
transparent electrode; and a counter electrode material layer
disposed on the second transparent electrode and contacting the
electrolyte solution.
[0008] In an embodiment, the counter electrode material layer may
include an ion storage material or an electrochromic material.
[0009] In an embodiment, the counter electrode material layer may
include at least one out of tungsten oxide (WO.sub.3), cerium oxide
(CeO.sub.2), titanium oxide (TiO.sub.2), nickel oxide (NiO),
molybdenum oxide (MoO.sub.3), cobalt oxide (CoO.sub.2), iridium
oxide (IrO.sub.2), and tin oxide (SnO.sub.2).
[0010] In an embodiment, the reversible electrochemical mirror may
further include a metal layer disposed on the first transparent
electrode and contacting the electrolyte solution.
[0011] In an embodiment, the electrolyte solution may include ions
of a metal included in the metal layer.
[0012] In an embodiment, the metal layer may be silver (Ag) or
bismuth (Bi), and the electrolyte solution may include silver ions
or bismuth ions.
[0013] In an embodiment, the electrolyte solution may further
include lithium ions, and the lithium ions may bond with a material
forming the counter electrode material layer when a negative
voltage is applied to the second transparent electrode.
[0014] In an embodiment, the lithium ions may be separated from a
material forming the counter electrode material layer when a
negative voltage is applied to the first transparent electrode.
[0015] In an embodiment, the electrolyte solution may further
include at least one solvent selected from water, dimethyl
sulfoxide (DMSO), propylene carbonate, and ethylene glycol.
[0016] In an embodiment, the electrolyte solution may desirably not
include copper ions.
[0017] In an embodiment, the first and second transparent
electrodes may include ITO or FTO.
[0018] In an embodiment, when a negative voltage is applied to the
first transparent electrode, a metal layer may be electrodeposited
on the first transparent electrode such that the reversible
electrochemical mirror becomes a mirror state, and when a negative
voltage is applied to the second transparent electrode, the metal
layer may dissolve into the electrolyte solution such that the
reversible electrochemical mirror becomes a transparent state.
BRIEF DESCRIPTION OF THE FIGURES
[0019] FIG. 1 is a cross-sectional view of a reversible
electrochemical mirror according to an embodiment of the inventive
concept;
[0020] FIG. 2 illustrates an electrodeposition operation of the
reversible electrochemical mirrors in FIGS. 1 and 4;
[0021] FIG. 3 illustrates an erasure operation of the reversible
electrochemical mirror in FIG. 1;
[0022] FIG. 4 is a cross-sectional view of a reversible
electrochemical mirror according to another embodiment of the
inventive concept;
[0023] FIG. 5 illustrates an erasure operation of the reversible
electrochemical mirror in FIG. 4;
[0024] FIG. 6 is a graph showing the reflectance of a reversible
electrochemical mirror manufactured in a manufacturing example of
an embodiment of the inventive concept according to the wavelength
of light;
[0025] FIG. 7 is a graph showing reflectance change properties
measured by repeating dissolution and electrodeposition operations
of silver on a reversible electrochemical mirror manufactured in a
manufacturing example of an embodiment of the inventive concept;
and
[0026] FIG. 8 is a graph showing the change in reflectance with
time after placing a reversible electrochemical mirror manufactured
in a manufacturing example of an embodiment of the inventive
concept in a mirror state and then cutting off power.
DETAILED DESCRIPTION
[0027] Objects described above of the inventive concept, and other
objects, features, and advantages of the inventive concept can be
easily understood through exemplary embodiments related to the
accompanying drawings. The inventive concept may, however, be
embodied in different forms and should not be construed as limited
to the embodiments set forth herein. Rather, these embodiments are
provided so that this disclosure will be thorough and complete, and
will fully convey the scope of the inventive concept to those
skilled in the art.
[0028] Herein, when an element is referred to as being on another
element, it can be directly on the other element, or a third
element may be interposed therebetween. Moreover, in the drawings,
the thickness of elements is exaggerated for effective description
of the technical contents.
[0029] Embodiments described herein will be described with
reference to cross-sectional views and/or plan views that are
idealized exemplary figures. In the drawings, the thickness of
films and regions are exaggerated for effective description of the
technical contents. Thus, the form in the idealized exemplary
figures may be modified due to manufacturing techniques and/or
tolerances and the like. Therefore, embodiments of the inventive
concept are not limited to the particular forms illustrated herein,
but instead, include modifications introduced due to the
manufacturing process. For example, an etched region illustrated as
forming a right angle may be rounded or have a predetermined
curvature. Thus, regions exemplified in the drawings have features,
and the shape of the exemplified regions are for exemplifying
particular forms of regions in an element, and are not intended to
limit the scope of the inventive concept. It will be understood
that, although the terms first, second, etc. may be used in various
embodiments herein to describe various elements, these elements
should not be limited by these terms. These terms are only used to
distinguish one element from another element. Embodiments herein
also include their complementary embodiments.
[0030] The terminology used herein is for the purpose of describing
particular embodiments only and is not intended to be limiting of
the invention. As used herein, singular forms are intended to
include their plural forms as well, unless the context clearly
indicates otherwise. As used herein, the terms `comprise` and/or
`comprising` specify the presence of stated elements, and do not
preclude the presence or addition of one or more other
elements.
[0031] Hereinafter, the present invention will be explained in
detail with reference to the accompanying drawings
[0032] FIG. 1 is a cross-sectional view of a reversible
electrochemical mirror according to an embodiment of the inventive
concept.
[0033] Referring to FIG. 1, a reversible electrochemical mirror 100
according to an embodiment includes a first substrate 10 and a
second substrate 20, which face each other. The first substrate 10
and second substrate 20 may be transparent. For example, the first
substrate 10 and second substrate 20 may include glass or plastic.
A first transparent electrode 12 facing the second substrate 20 is
disposed on the first substrate 10. A second transparent electrode
22 facing the first substrate 10 is disposed on the second
substrate 20. The first transparent electrode 12 and second
transparent electrode 22 may include, for example, indium tin oxide
(ITO) or fluorine-doped tin oxide (FTO).
[0034] A counter electrode material layer 30 is disposed on the
second transparent electrode 22. The counter electrode material
layer 30 may face the first transparent electrode 12. The counter
electrode material layer 30 may include an ion storage material or
an electrochromic material. During operation of the reversible
electrochemical mirror 100, the ion storage material or
electrochromic material may participate in a reduction reaction or
oxidation reaction that involves receiving or letting go of ions
and electrons of an electrolyte solution 40. Here, although the
operation mechanism is the same, the ion storage material is able
to maintain a transparent state in both the reduction reaction and
the oxidation reaction, whereas the electrochromic material may
change color as a result of the reduction reaction or oxidation
reaction. When composed of the electrochromic material, the counter
electrode material layer 30, like colored glass, may be transparent
while displaying color. The counter electrode material layer 30 may
include at least one out of tungsten oxide (WO.sub.3), cerium oxide
(CeO.sub.2), titanium oxide (TiO.sub.2), nickel oxide (NiO),
molybdenum oxide (MoO.sub.3), cobalt oxide (CoO.sub.2), iridium
oxide (IrO.sub.2), and tin oxide (SnO.sub.2). The tungsten oxide
(WO.sub.3) and nickel oxide (NiO) may, for example, correspond to
the electrochromic material. The cerium oxide (CeO.sub.2) and
titanium oxide (TiO.sub.2) may, for example, correspond to the ion
storage material.
[0035] Although not shown, a partition wall or spacer may be
disposed between the first substrate 10 and second substrate 20.
Accordingly, there may be a space between the first transparent
electrode 12 and the counter electrode material layer 30, and the
space may be filled with the electrolyte solution 40. The first
transparent electrode 12 and the counter electrode material layer
30 may contact the electrolyte solution 40. The electrolyte
solution 40 may include silver ions (Ag.sup.+) or bismuth ions
(Bi.sup.3+). The electrolyte solution 40 may further include
lithium ions. Specifically, the electrolyte solution 40 may include
at least one solvent selected from water, dimethyl sulfoxide
(DMSO), propylene carbonate, and ethylene glycol. The electrolyte
solution 40 may further include silver nitrate (AgNO.sub.3) and
lithium bromide (LiBr) dissolved in the solvent. The silver nitrate
(AgNO.sub.3) and lithium bromide (LiBr) may dissolve and thereby be
ionized into silver ions (Ag.sup.+), bromide ions (Br.sup.-),
lithium ions (Li.sup.+), and nitrate ions (NO.sub.3.sup.-). The
electrolyte solution 40 may further include a polymer. The polymer
may function as an electrolyte stiffener. The polymer may be, for
example, polyvinyl butyral (PVB). The electrolyte solution 40 may
exclude copper ions.
[0036] The reversible electrochemical mirror 100 in FIG. 1 may be
in a transparent state when initially manufactured.
[0037] Operation of the reversible electrochemical mirror 100 in
FIG. 1 will be described. FIG. 2 illustrates an electrodeposition
operation of the reversible electrochemical mirrors in FIGS. 1 and
4. FIG. 3 illustrates an erasure operation of the reversible
electrochemical mirror in FIG. 1.
[0038] Referring to FIG. 2, in order for the reversible
electrochemical mirror 100 to become a mirror state, a negative
voltage may be applied to the first transparent electrode 12 and a
positive voltage may be applied to the second transparent voltage
22 in the reversible electrochemical mirror 100 in FIG. 1. A
positive electrodeposition voltage V1 may be applied to the second
transparent electrode 22 relative to the first transparent
electrode 12. Thus, in the state illustrated in FIG. 2, metal ions
in the electrolyte solution 40 may receive electrons from the first
transparent electrode 12, thereby being reduced and forming an
electrodeposited metal layer 52 on the first transparent electrode
12 as illustrated in FIG. 3. Accordingly, the reversible
electrochemical mirror 100 becomes a mirror state, and light L
incident through the first substrate 10 may be reflected at the
surface of the metal layer 52.
[0039] Referring to FIG. 3, in order for the reversible
electrochemical mirror 100 to become a transparent state, a
positive voltage may be applied to the first transparent electrode
12 and a negative voltage may be applied to the second transparent
electrode 22. A negative erasure voltage V2 may be applied to the
second transparent electrode 22 relative to the first transparent
electrode 12. As a result, the metal layer 52 in FIG. 2 may be
dissolved into the electrolyte solution 40. After a predetermined
amount of time, the metal layer 52 may be completely dissolved such
that the first transparent electrode 12 contacts the electrolyte
solution 40. The reversible electrochemical mirror 100 becomes the
transparent state, and light L incident through the first substrate
10 may pass through the reversible electrochemical mirror 100.
[0040] The electrodeposition operation in the reversible
electrochemical mirror 100 in FIG. 1 may proceed via reactions such
as those below when the counter electrode material layer 30 is
composed of tungsten oxide, the metal layer 52 is composed of
silver, and the electrolyte solution 40 includes silver nitrate
(AgNO.sub.3) and lithium bromide (LiBr).
AgBr n 1 - n + e - -> Ag ( s ) + nBr - : Ag electrodeposition (
reduction ) Reaction Formula 1 3 2 Br - -> 1 2 Br 3 - + e - :
oxidation of Br - Reaction Formula 2 ##EQU00001##
[0041] The reduction reaction of Reaction Formula 1 may occur on
the first transparent electrode 12, and the oxidation reaction of
Reaction Formula 2 may occur on the second transparent electrode
22.
[0042] Moreover, the erasure operation in the reversible
electrochemical mirror 100 in FIG. 2 may proceed via reactions such
as those below.
Ag ( s ) + nBr - + e - -> AgBr n 1 - n : dissolution of Ag (
oxidation ) Reaction Formula 3 1 2 Br 3 - + e - -> 3 2 Br - :
reduction of Br 3 - Reaction Formula 4 ##EQU00002##
[0043] The oxidation reaction of Reaction Formula 3 may occur on
the metal layer 52, and the reduction reaction of Reaction Formula
4 may occur on the second transparent electrode 22.
[0044] During the dissolution operation of silver (Ag), the counter
electrode material layer 30 may be reduced before the arrival of
Br.sub.3.sup.- ions, and perform the role of a mediator that
temporarily receives electrons generated upon Ag dissolution
(oxidation), and then slowly gives and receives Br.sub.3.sup.- ions
and electrons.
[0045] Typical reversible electrochemical mirrors do not include
the counter electrode material layer 30, and typical electrolyte
solutions include copper ions. In typical reversible
electrochemical mirrors, the copper ions receive electrons, thereby
being reduced from Cu.sup.2+ to Cu.sup.+ before the arrival of
Br.sub.3.sup.- to an electrode, and after Ag is dissolved, the
Br.sub.3.sup.- ions and Cu.sup.+ ions slowly exchange charges. In
the case of a typical reversible electrochemical mirror, when the
electrodeposition voltage is removed after an electrodeposition
operation, the copper ions in the electrolyte solution dissolve the
electrodeposited silver, thereby transforming the reversible
electrochemical mirror into a transparent state. For the typical
reversible electrochemical mirror to maintain a mirror state,
silver must be continuously electrodeposited to replenish the
losses to a silver thin film (corresponding to the metal layer 52)
caused by copper ions, and thus power is continuously consumed. In
this case, when the surface area of the reversible electrochemical
mirror becomes large, a voltage drop is formed between the edges
and central portion of the reversible electrochemical mirror, and
thus there is a limitation in that increasing the size of the
reversible electrochemical mirror is difficult.
[0046] However, in an embodiment of the inventive concept, the
counter electrode material layer 30 performs the role of a
temporary mediator that gives and receives Br.sub.3.sup.- ions and
electrons, and thus silver may be cleanly dissolved without the
presence of copper ions. Moreover, since the electrolyte solution
40 according to an embodiment of the inventive concept does not
include copper, silver dissolution caused by copper ions does not
occur, and thus the reversible electrochemical mirror according to
an embodiment of the inventive concept may consume less current and
exhibit better bistability (the ability to maintain a mirror state
when power is off) than typical reversible electrochemical
mirrors.
[0047] FIG. 4 is a cross-sectional view of a reversible
electrochemical mirror according to another embodiment of the
inventive concept.
[0048] Referring to FIG. 4, in a reversible electrochemical mirror
101 according to the present embodiment, a deposited metal layer
52a may be disposed on the first transparent electrode 12 in FIG.
1. The deposited metal layer 52a may face the counter electrode
material layer 30. The deposited metal layer 52a may be deposited
by a deposition operation, such as CVD, PVD, or sputtering, when
manufacturing the reversible electrochemical mirror 101. That is,
in the present embodiment, the deposited metal layer 52a may
already exist in a deposited state in an initial state of the
reversible electrochemical mirror 101 prior to operation. Thus, the
reversible electrochemical mirror 101 according to the present
embodiment, due to the deposited metal layer 52a, may be in a
mirror state in the initial state.
[0049] FIG. 5 illustrates an erasure operation of the reversible
electrochemical mirror in FIG. 4.
[0050] Referring to FIG. 5, in order for the reversible
electrochemical mirror 101 to become a transparent state, a
positive voltage may be applied to the first transparent electrode
12, and a negative voltage may be applied to the second transparent
electrode 22. A negative erasure voltage V3 may be applied to the
second transparent electrode 22 relative to the first transparent
electrode 12. As a result, the deposited metal layer 52a in FIG. 4
may be dissolved into the electrolyte solution 40. After a
predetermined amount of time, the deposited metal layer 52a may be
completely dissolved such that the first transparent electrode 12
contacts the electrolyte solution 40. The reversible electrolyte
mirror 101 becomes the transparent state, and light L incident
through the first substrate 10 may pass through the reversible
electrochemical mirror 101.
[0051] The erasure operation in the reversible electrochemical
mirror in FIG. 4 may proceed via reactions such as those below when
the counter electrode material layer 30 is composed of tungsten
oxide, the metal layer 52 is composed of silver, and the
electrolyte solution 40 includes silver nitrate (AgNO.sub.3) and
lithium bromide (LiBr).
x{Ag (s)+nBr.sup.-.fwdarw.AgBr.sub.n.sup.1-n+d.sup.-}: Ag
dissolution (oxidation) <Reaction Formula 5>
WO.sub.3+xLi.sup.++xe.sup.-.fwdarw.Li.sub.xWO.sub.3: reduction of O
<Reaction Formula 6>
[0052] In Reaction Formula 5, the silver (Ag) forming the deposited
metal layer 52a may dissolve and thereby change into silver ions
(Ag.sup.+) that form complex ions with bromide ions (Br.sup.-). In
Reaction Formula 6, a tungsten oxide film forming the counter
electrode material layer 30 may receive electrons from lithium ions
(Li.sup.+) in the electrolyte solution 40 and thereby bond with the
lithium ions (Li.sup.+). The tungsten oxide film bonded with the
lithium ions (Li.sup.+) may be blue. Here, the counter electrode
material layer 30 may change into a state 30a that has received
lithium ions and electrons that were inside the electrolyte
solution 40.
[0053] Referring to FIG. 2, in order for the reversible
electrochemical mirror 101 to become a mirror state, a negative
voltage may be applied to the first transparent electrode 12 and a
positive voltage may be applied to the second transparent electrode
22 in the reversible electrochemical mirror 101 in FIG. 5. A
positive electrodeposition voltage V1 may be applied to the second
transparent electrode 22 relative to the first transparent
electrode 12. Thus, in the state illustrated in FIG. 2, metal ions
in the electrolyte solution 40 may receive electrons from the first
transparent electrode 12, thereby being reduced and forming an
electrodeposited metal layer 52 on the first transparent electrode
12 as illustrated in FIG. 3. Accordingly, the reversible
electrochemical mirror 101 once again becomes a mirror state, and
light L incident through the first substrate 10 may be reflected at
the surface of the metal layer 52.
[0054] Here, the electrodeposition operation in the reversible
electrochemical mirror 101 in FIG. 4 may proceed via reactions such
as those below when the counter electrode material layer 30 is
composed of tungsten oxide, the metal layer 52 is composed of
silver, and the electrolyte solution includes silver nitrate
(AgNO.sub.3) and lithium bromide (LiBr).
Li.sub.xWO.sub.3.fwdarw.WO.sub.3+xLi.sup.++xe.sup.-: oxidation of
Li.sub.xWO.sub.3 <Reaction Formula 7>
x{AgBr.sub.n.sup.1-n+e.sup.-.fwdarw.Ag (s)+nBr.sup.-}: Ag
electrodeposition (reduction) <Reaction Formula 8>
[0055] In Reaction Formula 7, the application of a positive voltage
to the second transparent electrode 22 may cause the tungsten oxide
film bonded with the lithium ions to release electrons and lithium
ions into the electrolyte solution 40. Thus, lithium ions
(Li.sup.+) and electrons may be separated from the tungsten oxide
film and travel into the electrolyte solution 40. In Reaction
Formula 8, a negative voltage applied to the first transparent
electrode 12 causes the silver ions (Ag.sup.+) in the electrolyte
solution 40 to obtain electrons and be electrodeposited/re-formed
on the first transparent electrode 12. After all of the electrons
received by the tungsten oxide film via Reaction Formula 6 are
released into the electrolyte solution 40 via Reaction Formula 7,
the electrodeposition of silver no longer proceeds, and
electrodeposition stops. That is, even if the electrodeposition
voltage V1 continues to be applied, continued consumption of
current may not occur when electrodeposition is completed.
Moreover, even if power is cut off from the reversible
electrochemical mirror 101 following the silver electrodeposition
operation, self-erasure does not occur inside the electrolyte
solution 40. The oxidation/reduction reactions of Reaction Formulas
5 and 6, and the oxidation/reduction reactions of Reaction Formulas
7 and 8 may be almost completely reversible. The reversible
electrochemical mirror 101 of the present embodiment may have
excellent bistability.
[0056] In the reversible electrochemical mirror 101 in FIG. 4, a
pre-electrodeposited metal layer 52a is further included such that
the counter electrode material layer 30 may directly participate in
the exchange of charges required for reversible electrodeposition
reactions. Thus, since dissolution/electrodeposition reactions
occur without the intervention of Br.sub.3.sup.-, self-dissolution
caused by Br.sub.3.sup.- does not occur. Therefore, in the
reversible electrochemical mirror 101 in FIG. 4, there is no
current consumption caused by self-dissolution, and the reversible
electrochemical mirror 101 has excellent bistability. Moreover,
since silver dissolution and electrodeposition are not determined
by the diffusion of Br.sub.3.sup.-, fast operation speeds may be
achieved.
[0057] The manufacturing process of the reversible electrochemical
mirror in FIG. 4 is as follows. A first substrate 10 and a second
substrate 20 are prepared. A first transparent electrode 12 and a
second transparent electrode 22 are formed on the first substrate
10 and the second substrate 20, respectively. The first transparent
electrode 12 and second transparent electrode 22 may be formed as
ITO or FTO by a deposition, coating, or lamination process. A
deposited metal layer 52a may be formed on the first transparent
electrode 12 by a deposition process such as sputtering, chemical
vapor deposition (CVD), or physical vapor deposition (PVD). A
counter electrode material layer 30 may be formed on the second
transparent electrode 22 by a deposition process such as
sputtering, CVD, or PVD. The first substrate 10 and the second
substrate 20 may be arranged such that the deposited metal layer
52a and the counter electrode material layer 30 are facing each
other, and the first substrate 10 and second substrate 20 may be
attached or joined with a spacer or partition wall interposed
therebetween. An electrolyte solution 40 may be injected between
the deposited metal layer 52a and the counter electrode material
layer 30.
Manufacturing Example
[0058] Soda lime glass was used for the first substrate 10 and
second substrate 20, and an ITO thin film was used for the first
transparent electrode 12 and second transparent 22 in FIG. 4. 50 mM
of silver nitrate (AgNO.sub.3) and 1.0 M of lithium bromide (LiBr)
were dissolved in dimethyl sulfoxide (DMSO), and 10 wt % of
polyvinyl butyral (PVB) was added as a polymer to prepare an
electrolyte solution 40. Copper ions were not added to the
electrolyte solution 40. A tungsten oxide film (WO.sub.3) was
formed as a counter electrode material layer 30 on the second
transparent electrode 22. The tungsten oxide film (WO.sub.3) was
formed to a thickness of 1.8 m through a reactive sputtering
process using a tungsten target and a gas mixture of argon and
oxygen under a process pressure of 20 mTorr. A silver (Ag) thin
film was formed as a deposited metal layer 52a on the first
transparent electrode 12. The silver thin film was deposited by a
sputtering process using a silver (Ag) target and argon gas under a
process pressure of 5 mTorr. The surface resistance of the silver
thin film was 0.52 .OMEGA./square, which corresponds to a thickness
of about 30.5 nm, as converted using the resistivity of silver.
[0059] The reversible electrochemical mirror of the present
embodiment was obtained by preparing each of an electrode obtained
by depositing Ag on an indium tin oxide (ITO)-deposited substrate
and an electrode obtained by depositing WO.sub.3 on an indium tin
oxide-deposited substrate, interposing a spacer, attaching the
first substrate 10 and the second substrate 20, thereby forming an
empty space between the first substrate 10 and second substrate 20,
and filling the empty space with the electrolyte solution 40. The
spacer may have a thickness of about 120 m. The operating surface
area of the reversible electrochemical mirror manufactured as such
was about 2.34 cm.sup.2.
[0060] To place the reversible electrochemical mirror in a
transparent state, a voltage of +1.8 V was applied as an erasure
voltage V3 to the first transparent electrode 12 relative to the
second transparent electrode 22, thereby dissolving all of the
silver of the deposited metal layer 52a into the electrolyte
solution 40.
[0061] To place the reversible electrochemical mirror in a mirror
state, a voltage of -1.0 V was applied as an electrodeposition
voltage V1 to the first transparent electrode 12 relative to the
second transparent electrode 22, thereby electrodepositing silver
on the first transparent electrode 12.
[0062] The tungsten oxide film may be one of electrochromic
materials that change color as a result of oxidation/reduction. If
a transparent ion storage material, such as cerium oxide, which
does not display color even when oxidized/reduced is used for the
counter electrode material layer 30, the reversible electrochemical
mirror may have an extremely high reflectance in a transparent
state.
[0063] FIG. 6 is a graph showing the reflectance of the reversible
electrochemical mirror manufactured in the manufacturing example of
an embodiment of the inventive concept according to the wavelength
of light.
[0064] Referring to FIG. 6, the dashed line represents a mirror
state and the solid line represents a transparent state. It can be
observed through FIG. 6 that excellent mirror states and
transparent states may be reversibly formed at various wavelengths
of light.
[0065] FIG. 7 is a graph showing reflectance change properties
measured by repeating dissolution and electrodeposition operations
of silver on the reversible electrochemical mirror manufactured in
the manufacturing example of an embodiment of the inventive
concept.
[0066] Referring to FIG. 7, 500 nm, 550 nm, and 600 nm each refer
to a wavelength of light incident on the reversible electrochemical
mirror. Electrodeposition operations were carried out by applying
-1.0 V as the electrodeposition voltage V1 of the reversible
electrochemical mirror to the first transparent electrode 12 for 10
seconds, and dissolution operations were carried out by applying
+1.8 V as the erasure voltage V3 to the first transparent electrode
12 for 10 seconds. FIG. 7 shows the reflectance, measured while
repeating the electrodeposition and dissolution operations,
according to time. It can be observed through FIG. 7 that the
reversible electrochemical mirror according to embodiments of the
inventive concept exhibits extremely fast switching properties and
clearly distinct mirror and transparent states.
[0067] FIG. 8 is a graph showing the change in reflectance with
time after placing the reversible electrochemical mirror
manufactured in the manufacturing example of an embodiment of the
inventive concept in a mirror state and then cutting off power.
[0068] Referring to FIG. 8, the reversible electrochemical mirror
maintains a mirror state even after power has been cut off. In
particular, it is observed that a reflectance of at least 50% is
maintained for 1 hour for a wavelength of 600 nm. Thus, it can be
seen that the reversible electrochemical mirror according to
embodiments of the inventive concept has excellent bistability.
[0069] A reversible electrochemical mirror according to embodiments
of the inventive concept may have excellent bistability and fast
switching properties. Moreover, the reversible electrochemical
mirror according to embodiments of the inventive concept may be
operated at low power and may maintain a stable mirror state or
transparent state even when power is cut off. Thus, the surface
area of the reversible electrochemical mirror may be easily
increased.
* * * * *